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Sample GSM989626 Query DataSets for GSM989626
Status Public on Sep 30, 2013
Title miRNA-tumour-P95_rep1
Sample type RNA
 
Source name frozen_breast_tumour
Organism Homo sapiens
Characteristics pam50 subtype assignment: PAM50_Normal
patient id: P95
path. review % of tumour cells: 50
ihc_pr: 0
ihc_er: 0
ihc_her2: 0
node positive: TRUE
grade: 2
traditional histological type: NST
diag_tumour_size: 4
mets_dd_after_diagnosis: NA
death_dd_after_diagnosis: NA
mets_count: 0
cause_of_death: NA
age_at_diagnosis: 59
Extracted molecule total RNA
Extraction protocol Total RNA extraction from fresh-frozen samples was performed after tissue homogenization with Qiagen miRNeasy Mini Kit (Qiagen GmbH, Hilden, Germany) completed with optional on-column DNase digestion carried out by RNase-Free DNase Set (Qiagen GmbH).
Label Cy3
Label protocol Total RNA was dephosphorylated, denaturated and Cyanine3-pCp ligated according to the manufacturer’s instructions using miRNA Complete Labeling and Hyb Kit (Agilent Tech. Inc.).
 
Hybridization protocol Samples were hybridized to Agilent Human miRNA Microarray Rel12.0 (Agilent Tech. Inc.) at 55oC, for 20 hours according to the manufacturer’s instructions.
Scan protocol After washing microarray slides array scanning was performed by Agilent DNA Microarray Scanner G2565BA (Agilent Tech. Inc.).
Data processing Feature extraction and data processing was performed with default scenario for Agilent Human MiRNA Microarray Rel12.0 by Feature Extraction Software 9.5.3 (Agilent Tech. Inc.) to calculate gProcessed signal. miRNA data were then post-processed using the AgiMicroRna (www.aroma-project.org) R package. Quality of individual arrays was assessed by visual evaluation of RLE (relative log expression), NUSE (normalised unscaled standard error) and hierarchical clustering plots. Robust Multichip Analysis (RMA) methodology was used to remove the array signal background, followed by quantile normalisation to correct for inter-arrays global differences and by miRNA level summarisation. miRNAs not detected or having saturated signal in more than 10 samples were filtered out. Replicated samples for the same patient were averaged.
 
Submission date Aug 21, 2012
Last update date Feb 27, 2014
Contact name Emanuele de Rinaldis
E-mail(s) emanuele_derinaldis@merck.com
Organization name IRBM (MERCK)
Street address Via Pontina
City Pomezia(Rome)
ZIP/Postal code 00100
Country Italy
 
Platform ID GPL10850
Series (1)
GSE40267 miRNA analysis of triple-negative breast cancers in association with clinical and molecular phenotypes

Data table header descriptions
ID_REF
VALUE RMA processed Cy3 signal intensity from the AgiMicroRna (www.aroma-project.org) R package

Data table
ID_REF VALUE
bkv-miR-B1-5p 6.39329632
ebv-miR-BART12 6.467605624
ebv-miR-BART13 7.673146544
ebv-miR-BART16 6.347700944
ebv-miR-BART19-3p 6.384986694
ebv-miR-BHRF1-1 6.403108152
hcmv-miR-UL148D 6.373394204
hcmv-miR-UL70-3p 8.076557442
hcmv-miR-US33-5p 6.423338758
hcmv-miR-US4 6.813777748
hiv1-miR-H1 6.967111445
hiv1-miR-TAR-3p 6.607444743
hsa-let-7a 13.58225731
hsa-let-7a* 6.333000198
hsa-let-7b 14.06967015
hsa-let-7b* 6.474422305
hsa-let-7c 11.48799613
hsa-let-7d 9.859028792
hsa-let-7d* 6.397735393
hsa-let-7e 10.080403

Total number of rows: 475

Table truncated, full table size 11 Kbytes.




Supplementary file Size Download File type/resource
GSM989626_Agilent_252182711725_S01_miRNA_107_Sep09_1_3.txt.gz 1.9 Mb (ftp)(http) TXT
Processed data included within Sample table

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